Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K080888 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| BrainLab Radiotherapy Treatment Planning Software; Catalog number 20610 - Radiosurgery 3.0 Cata... | 2 | 09/20/2009 | Brainlab AG |
| iPlan RT is a radiation treatment planning system that is intended for use in stereotactic, conforma... | 2 | 01/15/2015 | Brainlab AG |
| iPlan RT Dose is a stereotactic radiation treatment planning system that is intended for use in ster... | 2 | 01/15/2015 | Brainlab AG |
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